However, the growing number of resistant cases is still a clinical concern.Liver lobe torsion (LLT) is an uncommon condition of unknown origin in dogs. Several reports describe the clinical features and outcome, but only few of them include the imaging characteristics of this disease. The aim of this descriptive case series was to describe the ultrasonographic (US) and multidetector-row computed tomographic (MDCT) features of LLT in a group of dogs. Five dogs were included in this single-center descriptive study, having both US, CT and surgical and histological confirmation of LLT available for review. Different US appearances have been found, both hypoechoic and hyperechoic liver lobes and heterogeneous mass-like lesions, with fluid and gas content. At three-phase MDCT examination, LLT appeared as fluid- and gas-filled lesions (consistent with abscess transformation), or as hypoattenuating hypovascular lobes. Two different vascular signs were also described whirl sign or vascular interruption were seen in all cases, allowing a correct pre-surgical diagnosis in all the cases presented. Multiphase MDCT was a helpful imaging method for the correct pre-surgical diagnosis of LLT in dogs, and its use in the suspected cases is therefore advisable.The human bone marrow (hBM) is a complex organ critical for hematopoietic and immune homeostasis, and where many cancers metastasize. Understanding the fundamental biology of the hBM in health and diseases remain difficult due to complexity of studying or manipulating the BM in humans. Accurate biomaterial-based in vitro models of the hBM microenvironment are critical to further our understanding of the BM-niche and advancing new clinical interventions. Here we report a unique, 96-well format, microfluidic hBM-on-a-chip that incorporates the endosteal, central marrow, and perivascular niches of the human BM. Osteogenic differentiation of donor human mesenchymal stromal cells (MSCs) produced robust mineralization on the bottom surface ("bone-like endosteal layer") of the device, and subsequent seeding of human endothelial cells and MSCs in a fibrin-collagen hydrogel network ("central marrow") on the top created an interconnected 3D microvascular network ("perivascular niche"). The 96-well format allows eight independent "chips" to be studied in one plate, thereby increasing throughput and reproducibility. We show that this complex, multi-niche microtissue accurately mimics hBM composition and microphysiology, while providing key insights on hematopoietic progenitor dynamics. Presence of the endosteal niche decreased the proliferation and increased maintenance of CD34+ hematopoietic stem cells (HSCs). Upon exposure to radiation, HSCs in the hBM-chips containing endosteal niches were less frequently apoptotic, suggesting a potentially radio-protective role of the osteoblast surface. Our methods and results provide a broad platform for creating complex, multi-niche, high-throughput microphysiological (MPS) systems. Specifically, this hBM-on-a-chip opens new opportunities in human bone marrow research and therapeutics development, and can be used to better understand normal and impaired hematopoiesis, and various hBM pathologies, including cancer and BM failures.Sunken oil is often difficult to detect, and few oil spill models are designed to locate and track such oil. Therefore, the multi-modal Bayesian inferential sunken oil model, SOSim (Subsurface Oil Simulator), was expanded in this work for use during emergency response and damage assessment. Rather than requiring hydrodynamic data as input, SOSim v2 accepts available field concentration data, along with default or custom bathymetric data, for inference of the location and trajectory of sunken oil. Novel aspects include inference based on bathymetry and the Coriolis Effect, by constructing a prior likelihood function from sampled bathymetric data, scaled proportionally with field concentration data. SOSim v2 is demonstrated versus field data on the ITB DBL-152 oil spill in the Gulf of Mexico, with sensitivity analysis. Results suggest that the inferential approach presented can be effective for modeling relatively slow-moving pollutant masses such as sunken oil, when field concentration data are available.The SARS-CoV-2 virus is causing COVID-19, an ongoing pandemic, with extraordinary global health, social, and political implications. Currently, extensive research and development efforts are aimed at producing a safe and effective vaccine. In the interim, small molecules are being widely investigated for antiviral effects. With respect to viral replication, the papain-like (PLpro) and main proteases (Mpro), are critical for processing viral replicase polypeptides. Further, the PLpro possesses deubiquitinating activity affecting key signalling pathways, including inhibition of interferon and innate immune antagonism. Therefore, inhibition of PLpro activity with small molecules is an important research direction. Our aim was to focus on identification of potential inhibitors of the protease activity of SARS-CoV-2 PLpro. https://www.selleckchem.com/products/abtl-0812.html We investigated 300 small compounds derived predominantly from our OliveNet™ library (222 phenolics) and supplemented with synthetic and dietary compounds with reported antiviral activities. An initial docking screen, using the potent and selective noncovalent PLpro inhibitor, GRL-0617 as a control, enabled a selection of 30 compounds for further analyses. From further in silico analyses, including docking to scenes derived from a publicly available molecular dynamics simulation trajectory (100 μs PDB 6WX4; DESRES-ANTON-11441075), we identified lead compounds for further in vitro evaluation using an enzymatic inhibition assay measuring SARS-CoV-2 PLpro protease activity. Our findings indicate that hypericin possessed inhibition activity, and both rutin and cyanidin-3-O-glucoside resulted in a concentration-dependent inhibition of the PLpro, with activity in the micromolar range. Overall, hypericin, rutin, and cyanidin-3-O-glucoside can be considered lead compounds requiring further characterisation for potential antiviral effects in appropriate model systems.